Mb. Fallon et al., COMMON BILE-DUCT LIGATION IN THE RAT - A MODEL OF INTRAPULMONARY VASODILATATION AND HEPATOPULMONARY SYNDROME, American journal of physiology: Gastrointestinal and liver physiology, 35(4), 1997, pp. 779-784
Hepatopulmonary syndrome (HPS) causes impaired oxygenation due to intr
apulmonary vasodilatation in patients with cirrhosis. Chronic common b
ile duct ligation (CBDL) in the rat results in gas-exchange abnormalit
ies similar to HPS, but intrapulmonary vasodilatation has not been eva
luated. We assess intrapulmonary vasodilatation, measured in vivo, aft
er CBDL. Sham, 2- and 5-wk CBDL, and 3-wk partial portal vein ligated
(PVL) rats had hepatic and lung injury, portal. pressure, and arterial
blood gases assessed. The pulmonary microcirculation was evaluated by
injecting microspheres (size range 5.5-10 mu m) intravenously and mea
suring the size and number of microspheres bypassing the lungs in arte
rial blood. CBDL animals developed progressive hepatic injury and port
al hypertension accompanied by gas-exchange abnormalities and intrapul
monary vasodilatation. PVL animals, with a similar degree of portal hy
pertension, did not develop intrapulmonary vasodilatation or abnormal
gas exchange. No lung injury was observed. CBDL, but not PVL, causes p
rogressive intrapulmonary vasodilatation, which accompanies worsening
arterial gas exchange. These findings validate CBDL as a model to stud
y HPS.